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The Ct data was determined with default threshold settings.
Normal distribution of data was determined with Shapiro-Wilk test.
The evolutionary model fitting best the protein data was determined with ProtTest 1.2.6 with deactivated "+F" option [ 80, 81].
Prior to ML analysis, the model of molecular evolution best fitting to the data was determined with Modeltest version 3.5 [ 51].
The evolutionary model fitting best the data was determined with ProtTest 1.2.6 according to the AIC [ 45, 46] and used for maximum likelihood analysis with Phyml 2.4.4 [ 47].
Analysis of data was determined with BD Accuri CFlow software (set at 480 nm and 525 nm excitation and emission wavelengths, respectively).
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Similarly, this data are determined with greater precision and consistency.
Data were determined with high reliability and reproducibility and found to show considerable differences among the dedicated compounds ranging from 0.97 ± 0.37 up to 4.85 ± 0.01.
Because of the large spread of these values and because experimental data are determined with very big errors, it has been decided to obtain the VBO by another ab initio procedure.
Correlations between compositional and functional data were determined with the use of Pearson product moment estimates.
HRMS data were determined with a Bruker APEX-Q IV 7T spectrometer.
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